1<p>Mutations introduced in the first or second 12-residue metal binding loops of HsCen3 are indicated in bold and are underlined.</p>2<p>The dissociation constant (<i>K</i><sub>d</sub>) for each variant's Mg<sup>2+</sup> and first Ca<sup>2+</sup> binding event is indicated, together with the standard error (SE).</p>3<p>A binding event's dynamic range (D.R.) is defined as the difference in emission ratio between the unbound and fully metal bound form divided by the emission ratio in the unbound form, multiplied by 100%.</p
The introduction of weak, hydrophobic interactions between fluorescent protein domains (FPs) can sub...
<p>(A). Left - sensorgrams, showing R1 (analyte) binding to <i>Pf</i>AMA1 3D7mut (immobilized). R1 c...
<p>Plots of the equilibrium binding response, normalized to the R<sub>max</sub> value (the ligand im...
<p>(A) Crystal structure (PDB code 2GGM) of HsCen2 in the calcium-bound, compact state. The typical ...
<p>(A) Normalized fluorescence emission spectra of MagFRET-1 at 0 and at 16 mM Mg<sup>2+</sup> after...
<p>Binding affinities (K<sub>D</sub>) of the single mutants for MD2 were measured from the associati...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
Abstract MerR metalloregulators are the central components of many biosensor platforms designed to r...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
<p>Binding affinity (K<sub>D</sub>) of IgG1 and v1 to mFcRn at pH 7.0 and pH 6.0, binding affinity (...
<p>Binding affinity to various ligands was compared using the quenching value (Q), as shown in <a hr...
<p>Equilibrium binding of Fc variants to human FcRn in avidity binding format.</p
<p>Affinity measurement of the humanized SEM120-IIIC1 variants as scFv-Fc against holotoxin BoNT/A1 ...
<p><i>A–C</i>, background-corrected SPR sensorgrams of defensins, each at 333 nM, binding to immobil...
The introduction of weak, hydrophobic interactions between fluorescent protein domains (FPs) can sub...
<p>(A). Left - sensorgrams, showing R1 (analyte) binding to <i>Pf</i>AMA1 3D7mut (immobilized). R1 c...
<p>Plots of the equilibrium binding response, normalized to the R<sub>max</sub> value (the ligand im...
<p>(A) Crystal structure (PDB code 2GGM) of HsCen2 in the calcium-bound, compact state. The typical ...
<p>(A) Normalized fluorescence emission spectra of MagFRET-1 at 0 and at 16 mM Mg<sup>2+</sup> after...
<p>Binding affinities (K<sub>D</sub>) of the single mutants for MD2 were measured from the associati...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
Abstract MerR metalloregulators are the central components of many biosensor platforms designed to r...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
Magnesium has important structural, catalytic and signaling roles in cells, yet few tools exist to i...
<p>Binding affinity (K<sub>D</sub>) of IgG1 and v1 to mFcRn at pH 7.0 and pH 6.0, binding affinity (...
<p>Binding affinity to various ligands was compared using the quenching value (Q), as shown in <a hr...
<p>Equilibrium binding of Fc variants to human FcRn in avidity binding format.</p
<p>Affinity measurement of the humanized SEM120-IIIC1 variants as scFv-Fc against holotoxin BoNT/A1 ...
<p><i>A–C</i>, background-corrected SPR sensorgrams of defensins, each at 333 nM, binding to immobil...
The introduction of weak, hydrophobic interactions between fluorescent protein domains (FPs) can sub...
<p>(A). Left - sensorgrams, showing R1 (analyte) binding to <i>Pf</i>AMA1 3D7mut (immobilized). R1 c...
<p>Plots of the equilibrium binding response, normalized to the R<sub>max</sub> value (the ligand im...